Abstract
Insertion sequence (IS) regions have been identified previously as a cause of strongly polar mutations in Escherichia coli and several bacteriophages. The present experiments indicate that genetically characterized IS regions occur on bacterial plasmid deoxyribonucleic acid (DNA) as both direct and inverted DNA sequence duplications. The DNA insertion which has been shown previously (Sharp et al., 1973) to control expression of tetracycline resistance in the R6-5 plasmid, and which occurs as directly and inversely repeated DNA sequences adjacent to the region believed to contain the tetracycline resistance gene, has been identified as IS3. A second genetically characterized insertion sequence (IS1) has been identified as a direct DNA duplication occurring at both junctions of the resistance transfer factor and R-determinant components of R6-5 and related plasmids. A model is presented for the reversible dissociation of resistance transfer factor and R-determinant components of co-integrate R plasmids at the sites of DNA sequence homology provided by the repeated IS regions.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference28 articles.
1. The stabilization of episomal integration by genetic inversion: a general hypothesis;Adelberg E. A.;Proc. Natl. Acad. Sci.,1972
2. U.S.A.
3. Genetic expression in bacteriophage A. Ill. Inhibition of Escherichia coli nucleic acid and protein synthesis during A development;Cohen S. N.;J. Mol. Biol.,1970
4. Recircularization and autonomous replication of a sheared R-factor. DNA segment in Escherichia coli transformants;Cohen S. N.;Proc. Natl. Acad. Sci. U.S.A.,1973
5. Transcription of complementary strands of phage ADNA in vivo and in vitro;Cohen S. N.;Proc. Natl. Acad. Sci. U.S.A.,1967
Cited by
151 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献